Pontocerebellar hypoplasia type 10
MONDO:0014349Any non-syndromic pontocerebellar hypoplasia in which the cause of the disease is a mutation in the CLP1 gene.
Also known as: CLP1 non-syndromic pontocerebellar hypoplasia, CLP1-related pontocerebellar hypoplasia, PCH10, non-syndromic pontocerebellar hypoplasia caused by mutation in CLP1, pontocerebellar hypoplasia, type 10
1 clinical trial for this condition and its sub-types.
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Disease
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Nervous system disorder
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Hereditary disease
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Human disease
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Developmental defect during embryogenesis
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Hereditary neurological disease
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Central nervous system malformation
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Disease of genetic or genomic mechanism
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Pontocerebellar hypoplasia
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